Careers

The Wasdell Group is always on the lookout for talented and passionate people to work with us. If you think you have the necessary skills and enthusiasm to build a career at one of our packaging, manufacturing, distribution or engineering sites then please send us your CV via the form below.


Current Vacancies

Swindon


Trainee QP

The Wasdell Group is one of the largest and most experienced pharmaceutical contract packaging suppliers to the healthcare industry in Europe. A fantastic opportunity has arisen at our Swindon facility for a Trainee QP to join our busy team.

Reporting directly to the Director of Regulatory Affairs & QP Services, the role of Trainee QP will provide leadership in the Quality Assurance involvement of batch review and certification; work with internal and external auditing teams; review new regulation implementation to the business and support new product introduction.

The successful candidate will have:

• Previous experience of working within a QA Manager’s role within the Pharmaceutical sector
• Working knowledge of cGMP and pharmaceutical manufacturing or packaging requirements
• Experience of assisting in MHRA/FDA inspections and client audits
• Experience of and competent in working with Microsoft office
• Eligibility to act as a QP following training (i.e. suitable life science degree)

A fully funded company training programme will be put in place for the successful candidate.

This is a full time permanent role. Hours of work are Monday to Friday 8 am to 5 pm.

For further information or to apply for this role, please email Claire Aitkenhead (HR Officer) or alternatively contact the HR Team on 0191 2645856.

CVs will not be accepted from agencies.


QA Officer

The Wasdell Group is one of the largest and most experienced pharmaceutical contract packaging suppliers to the healthcare industry in Europe. A fantastic opportunity has arisen at our Swindon facility for an experienced and enthusiastic QA Officer to join our busy team.

Reporting to the QA Manager, the QA Officer will support the Quality Team with control of documentation, quality agreements, support Batch Release activities with review of batch documentation and assist with internal / external audits, deviations and customer complaint investigations.

The successful candidate must be able to ensure accurate approval of documents and able to make timely and quality decisions on all matters relating to Quality, GMP and compliance.

Candidates will ideally have proven experience in a quality based role in the pharmaceutical industry or have experience of working within a GMP (Good Manufacturing Practice) environment.

This is a full time permanent role. Hours of work are Monday to Friday 8 am to 5 pm.

For further information or to apply for this role, please email Claire Aitkenhead (HR Officer) or alternatively contact the HR Team on 0191 2645856.

CVs will not be accepted from agencies.


Validation Officer

The Wasdell Group is one of the largest and most experienced pharmaceutical contract packaging suppliers to the healthcare industry in Europe. A fantastic opportunity has arisen at our Swindon site for an experienced and enthusiastic Validation Officer to join our team. The role will be based in Swindon with frequent travel expected to our Newcastle and Burnley sites.

This is a fantastic opportunity for the successful candidate to take responsibility for the management and maintenance of the Site Validation Master Plan, ensuring compliance of the plan with EU GMP. You will also be responsible for the generation, issuing and control of Validation Documentation (URS, IQ, OQ, PQ and Validation Reports)

This role will also include but is not limited to:
· Completion of CAPAs;
· Responsibility for site validation status, ensuring all facilities, systems, processes and equipment are maintained in a validated state;
· Planning and scheduling Validation activities;
· Validating and Qualifying activities on facilities, systems, processes and equipment;
· Generating Change Controls for the introduction of new equipment and changes in equipment/facilities/processes or systems.

The successful candidate will have:

· Experience and knowledge cGMP and regulatory requirements.
· A minimum of 2 years validation experience
· A degree in a scientific or engineering discipline or equivalent industry experience.

This is a full time permanent role working 8.00am – 5.00pm Monday to Friday.

For further information or to apply for this role, please email Claire Aitkenhead (HR Officer) or alternatively contact the HR Team on 0191 2645856.

CVs will not be accepted from agencies.


Quality Assurance Specialist Vacancy

The Wasdell Group is one of the largest and most experienced pharmaceutical contract packaging suppliers to the healthcare industry in Europe. A fantastic opportunity has arisen at our Swindon site for an experienced and enthusiastic Quality Assurance Specialist to join our team.

This is a fantastic opportunity for the successful candidate to maintain the quality systems, and take the lead on deliverance of new starter and refresher GMP training.

Responsibilities will include but will not be limited to CAPA, Change Controls, deviations, internal and external auditing and review of batch documentation.
Candidates must have experience in electronic quality management systems, having worked within a GMP environment and have experience of SOP approval.

This is a full time permanent role. Hours of work are Monday to Friday 8 am to 5 pm.

For further information or to apply for this role, please email Claire Aitkenhead (HR Officer) or alternatively contact the HR Team on 0191 2645856.

CVs will not be accepted from agencies.


Training & Development Manager

The Wasdell Group is one of the largest and most experienced pharmaceutical contract packaging suppliers to the healthcare industry in Europe. A fantastic opportunity has arisen at our Swindon facility for an experienced and enthusiastic Training & Development Manager to join our busy team.

The Training and Development Manager will identify training and development needs within the organisation through job analysis and regular consultation with senior management. Oversee and expand the company training matrix based on the needs of the organisation.

The successful candidate will also work with third parties to develop suitable content for training and deliver the training when appropriate.

Candidates will ideally have proven experience in a Training and Development role.

This is a full time permanent role. Hours of work are Monday to Friday 8 am to 5 pm.

For further information or to apply for this role, please email Claire Aitkenhead (HR Officer) or alternatively contact the HR Team on 0191 2645856.

No agencies please. CVs will not be accepted from agencies.

Send your CV via the form below.


Production Operators

The completion of work on the packaging lines, in line with the requirements of the Production Supervisor / Manager and documentation.

Various shift patterns available, 7 days a week.

For further information or to apply for this role, please email Claire Aitkenhead (HR Officer) or alternatively contact the HR Team on 0191 2645856.

Send your CV via the form below


Packaging Engineers

Duties include: Maintaining all machinery and equipment to the standards of safety, GMP compliance and peak operating performance in their designated area of responsibility. Working closely with production and Quality Assurance to ensure maximum output within the defined Quality Standards.

Various shift patterns available, 7 days a week.

For further information or to apply for this role, please email Claire Aitkenhead (HR Officer) or alternatively contact the HR Team on 0191 2645856.

No agencies please. CVs will not be accepted from agencies.

Send your CV via the form below.


Burnley


QA Officer Vacancy

The Wasdell Group is one of the largest and most experienced pharmaceutical contract packaging suppliers to the healthcare industry in Europe. A fantastic opportunity has arisen at our Burnley facility for a QA Officer to join our busy team.

Reporting to the QA Team Leader, the QA Officer will support the Quality Team by maintaining the quality management system and SOP process. The role will also include releasing non-medical products, assisting with validation activities, reviewing batch documentation and assisting with deviations and customer complaint investigations.

The successful candidate will be a team player and have excellent attention to detail, ensuring accurate approval of documents as well as have the ability to make timely and quality decisions on all matters relating to Quality, GMP and compliance.

Candidates will ideally have some experience in a quality based role in the pharmaceutical industry / GMP.

This is a full time permanent role. Hours of work are Monday to Friday 8 am to 5 pm.

For further information or to apply for this role, please email Claire Aitkenhead (HR Officer) or alternatively contact the HR Team on 0191 2645856.

CVs will not be accepted from agencies.


Production Operators

The completion of work on the packaging lines, in line with the requirements of the Production Supervisor / Manager and documentation.

Working hours are on 2 shift, 06.00-14.00hrs and 14.00-22.00hrs, Monday to Friday.

Send your CV via the form below


Packaging Engineers

Duties include: Maintaining all machinery and equipment to the standards of safety, GMP compliance and peak operating performance in their designated area of responsibility. Working closely with production and Quality Assurance to ensure maximum output within the defined Quality Standards.

Working hours are on 2 shift, 06.00-14.00hrs and 14.00-22.00hrs, Monday to Friday.

For further information or to apply for this role, please email Claire Aitkenhead (HR Officer) or alternatively contact the HR Team on 0191 2645856.

No agencies please. CVs will not be accepted from agencies.

Send your CV via the form below.


Newcastle


Quality Assurance Manager

Reporting to the Group Head of Quality, responsibilities include:

Overall responsibility for the maintenance of GMP Standards at the Newcastle facility including: ensuring that packaging materials meet required standard; timely approval of documentation; batch release of Investigational Medicinal Products and ‘Specials’; GMP Certification of Licensed Medicinal Products; and maintaining the Newcastle site’s Quality System.

The QA Manager will: liaise with customers regarding technical agreements, manage the audit programme, audit suppliers, investigate customer complaints and manage the QA and QC teams based in Newcastle.

Candidates will ideally have proven experience in a quality based role in the pharmaceutical industry / GMP role and experience in a management / supervisory role.
No agencies please. CVs will not be accepted from agencies.

For further information or to apply for this role, please email Claire Aitkenhead (HR Officer) or alternatively contact the HR Team on 0191 2645856.

Send your CV via the form below



Location of role: SwindonBurnleyNewcastle

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